Clinical Affairs

2 days ago


Chennai, Tamil Nadu, India Meshira luxury Full time ₹ 4,59,840 - ₹ 6,27,040 per year
  • Age limit:20 to 30.
  • Clinical Study Design & Execution: Leading the design and implementation of clinical study protocols and monitoring their progress.
  • Regulatory Compliance: Ensuring all activities, from clinical trials to post-market evaluations, adhere to regulatory requirements and guidelines (e.g., FDA regulations, GCP).
  • Data Management & Analysis: Overseeing the collection, interpretation, and reporting of clinical data to ensure its accuracy and integrity.
  • Cross-Functional Collaboration: Working with various departments, including R&D, regulatory affairs, quality, risk management, and marketing, to integrate clinical strategy with product development.
  • Investigator & Site Management: Recruiting and managing relationships with clinical trial investigators and research sites.
  • Regulatory Submissions: Preparing the clinical sections of documents for regulatory submissions and providing clinical information for other reports.
  • Product Lifecycle Support: Providing scientific evidence and insights throughout the product's lifecycle, including during post-market surveillance.

Job Types: Full-time, Permanent, Fresher

Pay: ₹38, ₹52,536.72 per month

Benefits:

  • Food provided

Work Location: In person



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